CY1119804T1 - Συντηγμενες τετρα- ή πεντα-κυκλικες διϋδροδιαζεπινοκαρβαζολονες ως αναστολεις parp - Google Patents

Συντηγμενες τετρα- ή πεντα-κυκλικες διϋδροδιαζεπινοκαρβαζολονες ως αναστολεις parp

Info

Publication number
CY1119804T1
CY1119804T1 CY20171101198T CY171101198T CY1119804T1 CY 1119804 T1 CY1119804 T1 CY 1119804T1 CY 20171101198 T CY20171101198 T CY 20171101198T CY 171101198 T CY171101198 T CY 171101198T CY 1119804 T1 CY1119804 T1 CY 1119804T1
Authority
CY
Cyprus
Prior art keywords
tetra
cyclic
pythrodiazepinocarbasolones
parp
suspensions
Prior art date
Application number
CY20171101198T
Other languages
Greek (el)
English (en)
Inventor
Changyou Zhou
Bo REN
Hexiang Wang
Original Assignee
Beigene, Ltd.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Beigene, Ltd. filed Critical Beigene, Ltd.
Publication of CY1119804T1 publication Critical patent/CY1119804T1/el

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/06Peri-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/55Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • A61K31/551Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/55Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • A61K31/551Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
    • A61K31/55131,4-Benzodiazepines, e.g. diazepam or clozapine
    • A61K31/55171,4-Benzodiazepines, e.g. diazepam or clozapine condensed with five-membered rings having nitrogen as a ring hetero atom, e.g. imidazobenzodiazepines, triazolam
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/12Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains three hetero rings
    • C07D471/16Peri-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/22Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed systems contains four or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/12Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains three hetero rings
    • C07D487/14Ortho-condensed systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Epidemiology (AREA)
  • Rheumatology (AREA)
  • Engineering & Computer Science (AREA)
  • Pain & Pain Management (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Immunology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
  • Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
CY20171101198T 2011-12-31 2017-11-16 Συντηγμενες τετρα- ή πεντα-κυκλικες διϋδροδιαζεπινοκαρβαζολονες ως αναστολεις parp CY1119804T1 (el)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/CN2011/085148 WO2013097225A1 (en) 2011-12-31 2011-12-31 Fused tetra or penta-cyclic dihydrodiazepinocarbazolones as parp inhibitors

Publications (1)

Publication Number Publication Date
CY1119804T1 true CY1119804T1 (el) 2018-06-27

Family

ID=48696280

Family Applications (1)

Application Number Title Priority Date Filing Date
CY20171101198T CY1119804T1 (el) 2011-12-31 2017-11-16 Συντηγμενες τετρα- ή πεντα-κυκλικες διϋδροδιαζεπινοκαρβαζολονες ως αναστολεις parp

Country Status (29)

Country Link
US (4) US9260440B2 (enExample)
EP (2) EP3315500B1 (enExample)
JP (1) JP6034877B2 (enExample)
KR (1) KR101716012B1 (enExample)
CN (2) CN103703004B (enExample)
AU (1) AU2011384858B2 (enExample)
BR (1) BR112014012628B8 (enExample)
CA (1) CA2856309C (enExample)
CY (1) CY1119804T1 (enExample)
DK (1) DK2797921T3 (enExample)
EA (1) EA027533B1 (enExample)
ES (1) ES2645814T3 (enExample)
HR (1) HRP20171883T1 (enExample)
HU (1) HUE035153T2 (enExample)
IL (1) IL233365A (enExample)
IN (1) IN2014DN06169A (enExample)
LT (1) LT2797921T (enExample)
ME (1) ME02855B (enExample)
MX (1) MX353578B (enExample)
NO (1) NO2797921T3 (enExample)
NZ (1) NZ624063A (enExample)
PL (1) PL2797921T3 (enExample)
PT (1) PT2797921T (enExample)
RS (1) RS56616B1 (enExample)
SG (1) SG11201401726VA (enExample)
SI (1) SI2797921T1 (enExample)
SM (1) SMT201700543T1 (enExample)
WO (1) WO2013097225A1 (enExample)
ZA (1) ZA201405560B (enExample)

Families Citing this family (33)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NO2797921T3 (enExample) 2011-12-31 2018-02-03
WO2013132253A1 (en) 2012-03-07 2013-09-12 Institute Of Cancer Research: Royal Cancer Hospital (The) 3-aryl-5-substituted-isoquinolin-1-one compounds and their therapeutic use
EP3044221B1 (en) 2013-09-11 2018-02-21 Institute of Cancer Research: Royal Cancer Hospital (The) 3-aryl-5-substituted-isoquinolin-1-one compounds and their therapeutic use
IL257442B2 (en) 2015-08-25 2023-03-01 Beigene Ltd Process for preparing parp inhibitor, crystalline forms and their uses
US20190142811A1 (en) * 2016-04-01 2019-05-16 Zeno Royalties & Milestones, LLC Estrogen receptor modulators
WO2018059437A1 (en) 2016-09-27 2018-04-05 Beigene, Ltd. Treatment cancers using combination comprising parp inhibitors
WO2018157794A1 (en) * 2017-02-28 2018-09-07 Beigene, Ltd. Crystalline forms of salts of fused tera or penta-cyclic dihydrodiazepinocarazolones, and uses thereof
CN106883232B (zh) * 2017-03-31 2019-01-22 苏州康润医药有限公司 一种氮杂非那烯-3-酮的衍生物及其制备方法与应用
US20200155567A1 (en) * 2017-07-17 2020-05-21 Beigene, Ltd. Treatment of cancers using a combination comprising parp inhibitors, temozolomide and/or radiation therapy
AU2019275722A1 (en) * 2018-06-01 2020-11-12 Beigene, Ltd. Maintenance therapy of a PARP inhibitor in treating gastric cancer
CN111171031B (zh) * 2019-05-10 2021-04-09 百济神州(苏州)生物科技有限公司 一种含parp抑制剂倍半水合物产物的制备方法
CN111171002B (zh) * 2019-05-16 2021-04-06 百济神州(苏州)生物科技有限公司 一种parp抑制剂中间体的制备方法
EA202192272A1 (ru) 2019-05-31 2022-03-02 Бейджин, Лтд. Гранулированный препарат ингибитора parp и способ его получения
EP3993787A4 (en) 2019-08-06 2023-07-12 Recurium IP Holdings, LLC Estrogen receptor modulators for treating mutants
WO2021046014A1 (en) 2019-09-03 2021-03-11 Teva Czech Industries S.R.O Solid state forms of pamiparib and process for preparation thereof
CN121712509A (zh) 2023-05-04 2026-03-20 锐新医药公司 用于ras相关疾病或病症的组合疗法
US20250049810A1 (en) 2023-08-07 2025-02-13 Revolution Medicines, Inc. Methods of treating a ras protein-related disease or disorder
IL327306A (en) 2023-10-12 2026-05-01 Revolution Medicines Inc Macrocyclic RAS inhibitors
WO2025171296A1 (en) 2024-02-09 2025-08-14 Revolution Medicines, Inc. Ras inhibitors
WO2025217307A1 (en) 2024-04-09 2025-10-16 Revolution Medicines, Inc. Methods for predicting response to a ras(on) inhibitor and combination therapies
WO2025240847A1 (en) 2024-05-17 2025-11-20 Revolution Medicines, Inc. Ras inhibitors
WO2025255438A1 (en) 2024-06-07 2025-12-11 Revolution Medicines, Inc. Methods of treating a ras protein-related disease or disorder
WO2025265060A1 (en) 2024-06-21 2025-12-26 Revolution Medicines, Inc. Therapeutic compositions and methods for managing treatment-related effects
WO2026006747A1 (en) 2024-06-28 2026-01-02 Revolution Medicines, Inc. Ras inhibitors
WO2026015790A1 (en) 2024-07-12 2026-01-15 Revolution Medicines, Inc. Methods of treating a ras related disease or disorder
WO2026015825A1 (en) 2024-07-12 2026-01-15 Revolution Medicines, Inc. Use of ras inhibitor for treating pancreatic cancer
WO2026015801A1 (en) 2024-07-12 2026-01-15 Revolution Medicines, Inc. Methods of treating a ras related disease or disorder
WO2026015796A1 (en) 2024-07-12 2026-01-15 Revolution Medicines, Inc. Methods of treating a ras related disease or disorder
WO2026050446A1 (en) 2024-08-29 2026-03-05 Revolution Medicines, Inc. Ras inhibitors
WO2026072904A2 (en) 2024-09-26 2026-04-02 Revolution Medicines, Inc. Compositions and methods for treating lung cancer
WO2026090116A2 (en) 2024-10-21 2026-04-30 Revolution Medicines, Inc. Ras inhibitors
WO2026090245A1 (en) 2024-10-22 2026-04-30 Revolution Medicines, Inc. Use of ras inhibitors for treating cancer
US20260108528A1 (en) 2024-10-22 2026-04-23 Revolution Medicines, Inc. Methods of treating a ras protein-related disease or disorder

Family Cites Families (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SE445326B (sv) 1983-04-05 1986-06-16 Malmstroem Anders E H Sett och anordning for forhindrande av veggturbulens
US6799298B2 (en) 1998-03-11 2004-09-28 Overture Services, Inc. Technique for locating an item of interest within a stored representation of data
EE05006B1 (et) 1999-01-11 2008-04-15 Agouron Pharmaceuticals, Inc. Polü(ADP-riboos)polümeraaside tritsüklilised inhibiitorid ja neid sisaldavad farmatseutilised kompositsioonid
MXPA03004832A (es) 2000-12-01 2004-05-04 Guilford Pharm Inc Compuestos y sus usos.
US6423705B1 (en) 2001-01-25 2002-07-23 Pfizer Inc. Combination therapy
US6906096B2 (en) 2002-06-28 2005-06-14 Irm Llc 4,7-Disubstituted indoles and methods of making
PL378372A1 (pl) 2003-01-09 2006-04-03 Pfizer Inc. Tricykliczne związki jako inhibitory kinaz białkowych do wzmacniania skuteczności środków przeciwnowotworowych i radioterapii
WO2004105700A2 (en) 2003-05-28 2004-12-09 Guildford Pharmaceuticals, Inc. Compounds, methods and pharmaceutical compositions for inhibiting parp
AU2007232279B2 (en) 2006-04-04 2010-05-06 Pfizer Products Inc. Combination therapy of (2R)-2-amino-2-cyclohexyl-N-(2-(1-methyl-1H-pyrazol-4-yl)-6- oxo-5,6-dihydro-1H-[1,2]diazepino[4,5,6-cd]indol-8-yl)acetamide
EP2004655A1 (en) 2006-04-04 2008-12-24 Pfizer Products Incorporated Polymorphic forms of (2r,z)-2-amino-2-cyclohexyl-n-(5-(1-methyl-1h-pyrazol-4 l)-1-oxo-2,6-dihydro-1h-ý1,2¨diazepinoý4,5,6-cd¨indol-8-yl)acetamide
WO2009063244A1 (en) 2007-11-15 2009-05-22 Istituto Di Ricerche Di Biologia Molecolare P. Angeletti S.P.A. Pyridazinone derivatives as parp inhibitors
US8012976B2 (en) * 2008-08-06 2011-09-06 Biomarin Pharmaceutical Inc. Dihydropyridophthalazinone inhibitors of poly(ADP-ribose)polymerase (PARP)
WO2011130661A1 (en) 2010-04-16 2011-10-20 Biomarin Pharmaceutical Inc. Methods of using dihydropyridophthalazinone inhibitors of poly (adp-ribose)polymerase (parp)
NO2797921T3 (enExample) 2011-12-31 2018-02-03
LT3702373T (lt) 2013-09-13 2022-11-10 Beigene Switzerland Gmbh Anti-pd1 antikūnai ir jų naudojimas terapijai ir diagnostikai
TWI726608B (zh) 2014-07-03 2021-05-01 英屬開曼群島商百濟神州有限公司 抗pd-l1抗體及其作為治療及診斷之用途
US9637488B2 (en) 2015-01-29 2017-05-02 Fuqiang Ruan Heterocyclic compounds as inhibitors of class I PI3KS
IL257442B2 (en) 2015-08-25 2023-03-01 Beigene Ltd Process for preparing parp inhibitor, crystalline forms and their uses
WO2018059437A1 (en) 2016-09-27 2018-04-05 Beigene, Ltd. Treatment cancers using combination comprising parp inhibitors
WO2018157794A1 (en) 2017-02-28 2018-09-07 Beigene, Ltd. Crystalline forms of salts of fused tera or penta-cyclic dihydrodiazepinocarazolones, and uses thereof
US20200155567A1 (en) 2017-07-17 2020-05-21 Beigene, Ltd. Treatment of cancers using a combination comprising parp inhibitors, temozolomide and/or radiation therapy

Also Published As

Publication number Publication date
NZ624063A (en) 2016-09-30
US20170305921A1 (en) 2017-10-26
PL2797921T3 (pl) 2018-02-28
US20160159811A1 (en) 2016-06-09
RS56616B1 (sr) 2018-02-28
DK2797921T3 (en) 2017-10-02
US20150175617A1 (en) 2015-06-25
AU2011384858A1 (en) 2014-05-29
SMT201700543T1 (it) 2018-01-11
CN103703004B (zh) 2016-06-29
JP6034877B2 (ja) 2016-11-30
KR101716012B1 (ko) 2017-03-13
HUE035153T2 (en) 2018-05-02
HK1192233A1 (zh) 2014-08-15
CN103703004A (zh) 2014-04-02
EP3315500B1 (en) 2020-03-18
ME02855B (me) 2018-04-20
MX353578B (es) 2018-01-19
WO2013097225A1 (en) 2013-07-04
ZA201405560B (en) 2017-02-22
SI2797921T1 (en) 2018-01-31
CA2856309A1 (en) 2013-07-04
US9260440B2 (en) 2016-02-16
EP2797921A4 (en) 2015-10-21
CA2856309C (en) 2016-06-07
MX2014007840A (es) 2014-08-21
BR112014012628B8 (pt) 2023-01-17
PT2797921T (pt) 2017-11-14
US20190016731A1 (en) 2019-01-17
US10501467B2 (en) 2019-12-10
IL233365A0 (en) 2014-08-31
IL233365A (en) 2016-08-31
US10112952B2 (en) 2018-10-30
US9617273B2 (en) 2017-04-11
NO2797921T3 (enExample) 2018-02-03
CN106220635A (zh) 2016-12-14
ES2645814T3 (es) 2017-12-07
CN106220635B (zh) 2019-03-08
EP2797921B1 (en) 2017-09-06
EA201491303A1 (ru) 2014-10-30
BR112014012628A2 (pt) 2017-06-13
EP3315500A1 (en) 2018-05-02
SG11201401726VA (en) 2014-10-30
KR20140107353A (ko) 2014-09-04
BR112014012628B1 (pt) 2021-02-09
HRP20171883T1 (hr) 2018-01-12
EP2797921A1 (en) 2014-11-05
IN2014DN06169A (enExample) 2015-08-21
EA027533B1 (ru) 2017-08-31
AU2011384858B2 (en) 2016-05-05
JP2015503526A (ja) 2015-02-02
LT2797921T (lt) 2017-11-27

Similar Documents

Publication Publication Date Title
MX353578B (es) Dihidrodiazpinocarbazolonas tetra o penta-ciclicas fusionadas como inhibidores de poli (adp-ribosa) polimerasa (parp).
EA201491304A1 (ru) Конденсированные тетра- или пентациклические пиридофталазиноны в качестве ингибиторов parp
UY34472A (es) Derivados modificados de 4-fenil-piridina
CY1118226T1 (el) Συγχωνευμενες τρικυκλικες ενωσεις ως αναστολεις κινασης raf
UY33925A (es) Inhibidores tricíclicos de quinasas
UY33985A (es) Sales de 2,3-dihidroimidazo [1,2-c] quinazolina sustituida
UY34602A (es) ?Derivados de bencimidazolil- e imidazopiridinil-metilamina?
UY33943A (es) Derivados espirocíclicos de isoxazolina como agentes antiparasitarios.
UY34550A (es) Bencilpirazoles sustituidos
SMT201600205B (it) DERIVATI BENZOTIOFENICI SOSTITUITI CON PIPERAZINA COME AGENTI ANTlPSICOTICI
UY33977A (es) Híbrido de pigmento autoaglutinante.
UY34374A (es) Benzilindazoles sustituidos
UY34885A (es) Proteínas de unión anti-mesotelina
UY34763A (es) Inhibidores de la agregación plaquetaria
UY34541A (es) ?derivados de dihidro-benzo-oxazina y dihidro-pirido-oxazina?.
UY34034A (es) Triazolopiridinas
CR20140079A (es) Aminoquinazolinas como inhibidores de quinasa
DK3524618T3 (da) Gla-domæner som targetteringsmidler
PL3321276T3 (pl) Białka fuzyjne do leczenia zaburzeń metabolicznych
UY34483A (es) Polipeptido
UY34158A (es) Composicion herbicida
FI20115328A7 (fi) Uusia kutinaaseja, niiden tuottaminen ja käytöt
ME02908B (me) Supstituisani 2-alkil-1-okso-n-fenil-3-heteroaril-1,2,3,4-tetrahidroizohinolin-4-karboksamidi za antimalarijske terapije
UY34032A (es) Nuevos inhibidores de quinasa
UY34099A (es) ?composición de agentes de coalescencia?.